Design of Marine Cyclodepsipeptide Analogues Targeting Candida albicans Efflux Pump CaCdr1p

• Type: Article in International Scientific Journal
• Date: 2024

Authors

Ribeiro, R (Author) Other; Fortes, S (Author) Other; Costa, L (Author) Other; Palmeira, A (Author) FFUP; Eugenia Pinto (Author) FFUP; Emilia Sousa (Author) FFUP; Carla Fernandes (Author) FFUP

Journal

Title: Drugs and Drug Candidates

Vol. 25

Pages: 537-549

Publisher: MDPI

Other information

Authenticus ID: P-011-6CY

DOI: 10.3390/ddc3030031

Abstract (EN): <jats:p>Fungal infections are a significant threat to human health and the environment. The emergence of multidrug-resistant strains of fungi and the growing prevalence of azole resistance in invasive fungal infections exacerbate the problem, with efflux pumps being a major cause of antifungal resistance and a prime target for several counteractive strategies. In Candida albicans, the ATP-binding cassette superfamily transporter CaCdr1p is the predominant efflux pump involved in azole resistance. Marine organisms have unique phenotypic characteristics to survive in challenging environments, resulting in biologically active compounds. The cyclodepsipeptides unnarmicin A and C have shown promising results as inhibitors of rhodamine 6G efflux in cells expressing CaCdr1p. Herein, a series of unnarmicin analogues were designed and docked against a CaCdr1p efflux pump based on the cryogenic electron microscopy structure available to select the most promising compounds. Analogue 33 was predicted to be the best considering its high affinity for the efflux pump and pharmacokinetic profile. These results pave the way for further synthesis and in vitro biological studies of novel unnarmicins seeking a synergistic effect with fluconazole.</jats:p>

Language: English

Type (Professor's evaluation): Scientific